BR9510490A - Combined two-component system designed for use in a mustard ribonucleotide host pharmaceutical composition half component mutant enzyme process to control neoplastic cell growth in a plasmid host vector and cell polynucleotide sequence - Google Patents

Combined two-component system designed for use in a mustard ribonucleotide host pharmaceutical composition half component mutant enzyme process to control neoplastic cell growth in a plasmid host vector and cell polynucleotide sequence

Info

Publication number
BR9510490A
BR9510490A BR9510490A BR9510490A BR9510490A BR 9510490 A BR9510490 A BR 9510490A BR 9510490 A BR9510490 A BR 9510490A BR 9510490 A BR9510490 A BR 9510490A BR 9510490 A BR9510490 A BR 9510490A
Authority
BR
Brazil
Prior art keywords
host
component
enzyme
prodrug
natural
Prior art date
Application number
BR9510490A
Other languages
Portuguese (pt)
Other versions
BR9510490B1 (en
Inventor
Christopher John Taylerson
Hendrikus Johannes Eggelte
Antonio Tarragona-Fiol
Brian Robert Rabin
Francis Thomas Boyle
John Frederick Hennam
David Charles Blakey
Peter Robert Marsham
David William Heaton
David Huw Davies
Anthony Michael Slater
Laurent Francois And Hennequin
Original Assignee
Zeneca Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26306259&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=BR9510490(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from GBGB9426192.2A external-priority patent/GB9426192D0/en
Priority claimed from GBGB9516810.0A external-priority patent/GB9516810D0/en
Application filed by Zeneca Ltd filed Critical Zeneca Ltd
Publication of BR9510490A publication Critical patent/BR9510490A/en
Publication of BR9510490B1 publication Critical patent/BR9510490B1/en

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6891—Pre-targeting systems involving an antibody for targeting specific cells
    • A61K47/6899—Antibody-Directed Enzyme Prodrug Therapy [ADEPT]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)

Abstract

PCT No. PCT/GB95/02991 Sec. 371 Date Jun. 23, 1997 Sec. 102(e) Date Jun. 23, 1997 PCT Filed Dec. 21, 1995 PCT Pub. No. WO96/20011 PCT Pub. Date Jul. 4, 1996A two component system for therapeutic treatment of a host, having a first component comprising a targeting moiety capable of binding with a tumour associated antigen, linked to a mutated enzyme capable of converting a prodrug into an antineoplastic drug, and a second component comprising a prodrug convertible under the influence of the mutated enzyme to the antineoplastic drug. The mutated enzyme is a mutated form of a natural host enzyme which recognizes its natural substrate by an ion pair interaction with the substrate, wherein the mutated enzyme and prodrug have structures such that the polarity of the mutated enzyme/prodrug ion pair interaction is reversed relative to the natural host enzyme/natural substrate ion pair interaction. The first component is substantially non-immunogenic in the host and the prodrug second component is not significantly convertible into antineoplastic drug in the host by natural unmutated host enzyme.
BRPI9510490-9A 1994-12-23 1995-12-21 structured two-component combined pharmaceutical composition for use in a host. BR9510490B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB9426192.2A GB9426192D0 (en) 1994-12-23 1994-12-23 Chemical compounds
GBGB9516810.0A GB9516810D0 (en) 1995-08-16 1995-08-16 Chemical compounds
PCT/GB1995/002991 WO1996020011A1 (en) 1994-12-23 1995-12-21 Chemical compounds

Publications (2)

Publication Number Publication Date
BR9510490A true BR9510490A (en) 1998-01-13
BR9510490B1 BR9510490B1 (en) 2010-10-05

Family

ID=26306259

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI9510490-9A BR9510490B1 (en) 1994-12-23 1995-12-21 structured two-component combined pharmaceutical composition for use in a host.

Country Status (23)

Country Link
US (1) US5985281A (en)
EP (1) EP0806964B1 (en)
JP (1) JP3805365B2 (en)
KR (1) KR100270650B1 (en)
CN (1) CN1095677C (en)
AT (1) ATE222124T1 (en)
AU (1) AU701916B2 (en)
BR (1) BR9510490B1 (en)
CA (1) CA2205091A1 (en)
CZ (1) CZ195297A3 (en)
DE (1) DE69527805T2 (en)
ES (1) ES2181805T3 (en)
FI (1) FI972683A0 (en)
HU (1) HUT77450A (en)
IL (1) IL116511A0 (en)
MX (1) MX9704575A (en)
NO (1) NO972882L (en)
NZ (1) NZ297529A (en)
PL (1) PL184031B1 (en)
RU (1) RU2189251C2 (en)
SK (1) SK80997A3 (en)
TR (1) TR199501654A2 (en)
WO (1) WO1996020011A1 (en)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0844885A2 (en) * 1995-08-16 1998-06-03 Zeneca Limited Chemical compounds
SG71046A1 (en) 1996-10-10 2000-03-21 Connector Systems Tech Nv High density connector and method of manufacture
AU6000698A (en) * 1997-02-14 1998-09-08 Zeneca Limited Proteins
GB9703201D0 (en) * 1997-02-15 1997-04-02 Zeneca Ltd Chemical compounds
GB9709421D0 (en) * 1997-05-10 1997-07-02 Zeneca Ltd Chemical compounds
US20040117863A1 (en) * 1998-09-18 2004-06-17 Edge Michael D. Transgenically produced fusion proteins
US6361774B1 (en) 1999-09-17 2002-03-26 Immunomedics, Inc. Methods and compositions for increasing the target-specific toxicity of a chemotherapy drug
AU763628B2 (en) * 1998-09-18 2003-07-31 Immunomedics Inc. Methods and compositions for increasing the target-specific toxicity of a chemotherapy drug
RU2002110121A (en) * 1999-09-17 2004-03-10 Джитиси Байотерапьютикс, Инк. (Us) Fused Proteins Obtained by Transgenic Method
EP1565564A4 (en) * 2002-11-27 2006-06-07 Gtc Biotherapeutics Inc Modified antibodies stably produced in milk and methods of producing same
US20080019905A9 (en) * 2005-02-18 2008-01-24 Strome Scott E Method of using an anti-CD137 antibody as an agent for radioimmunotherapy or radioimmunodetection
ES2417147T3 (en) * 2005-10-21 2013-08-06 Revo Biologics, Inc. Antibodies with enhanced antibody dependent cell cytotoxicity activity, methods for their production and use
US20080031866A1 (en) * 2006-06-20 2008-02-07 Eichenbaum Gary M Method for modulating the pharmacokinetics and metabolism of a therapeutic agent
WO2007149827A2 (en) * 2006-06-20 2007-12-27 Janssen Pharmaceutica, N.V. Method for modulating the pharmacokinetics and metabolism of a therapeutic agent
EP2792670A1 (en) 2006-10-03 2014-10-22 Techfields Biochem Co. Ltd Positively charged water-soluble prodrugs of mustards and related compounds with very high skin penetration rates
GB0709333D0 (en) * 2007-05-15 2007-06-20 Smart Targeting Ltd Binding protein
EP2279003A4 (en) * 2008-05-01 2013-04-03 Gtc Biotherapeutics Inc An anti-cd137 antibody as an agent in the treatment of inflammatory conditions
US10745492B1 (en) 2019-04-03 2020-08-18 Ark Diagnostics, Inc. Antibodies to symmetrically dimethylated arginine analytes and use thereof

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8705477D0 (en) * 1987-03-09 1987-04-15 Carlton Med Prod Drug delivery systems
US4975278A (en) * 1988-02-26 1990-12-04 Bristol-Myers Company Antibody-enzyme conjugates in combination with prodrugs for the delivery of cytotoxic agents to tumor cells
US5632990A (en) * 1988-04-22 1997-05-27 Cancer Research Campaign Tech. Ltd. Treatment for tumors comprising conjugated antibody A5B7 and a prodrug
GB8809616D0 (en) * 1988-04-22 1988-05-25 Cancer Res Campaign Tech Further improvements relating to drug delivery systems
US5433955A (en) * 1989-01-23 1995-07-18 Akzo N.V. Site specific in vivo activation of therapeutic drugs
EP0454783B1 (en) * 1989-01-23 1995-06-07 Akzo Nobel N.V. Site specific in-vivo activation of therapeutic drugs
AU674137B2 (en) * 1992-01-30 1996-12-12 Genzyme Limited Chiral synthesis with modified enzymes
GB9323429D0 (en) * 1993-11-12 1994-01-05 Wellcome Found Therapy
US5389537A (en) * 1994-01-21 1995-02-14 Wisconsin Alumni Research Foundation Nuclease having altered specificity

Also Published As

Publication number Publication date
TR199501654A2 (en) 1996-07-21
PL320964A1 (en) 1997-11-24
CN1171054A (en) 1998-01-21
NO972882D0 (en) 1997-06-20
KR100270650B1 (en) 2000-11-01
DE69527805D1 (en) 2002-09-19
AU4269796A (en) 1996-07-19
WO1996020011A1 (en) 1996-07-04
EP0806964A1 (en) 1997-11-19
ATE222124T1 (en) 2002-08-15
DE69527805T2 (en) 2003-04-24
BR9510490B1 (en) 2010-10-05
NO972882L (en) 1997-08-19
NZ297529A (en) 1999-07-29
CZ195297A3 (en) 1997-12-17
FI972683A (en) 1997-06-19
US5985281A (en) 1999-11-16
RU2189251C2 (en) 2002-09-20
PL184031B1 (en) 2002-08-30
AU701916B2 (en) 1999-02-11
ES2181805T3 (en) 2003-03-01
JP3805365B2 (en) 2006-08-02
FI972683A0 (en) 1997-06-19
CA2205091A1 (en) 1996-07-04
EP0806964B1 (en) 2002-08-14
JPH10511547A (en) 1998-11-10
HUT77450A (en) 1998-04-28
SK80997A3 (en) 1998-02-04
MX9704575A (en) 1997-10-31
CN1095677C (en) 2002-12-11
TR199501654A3 (en) 1996-07-21
IL116511A0 (en) 1996-07-23

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